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男性和女性内源性孕激素和雌激素与葡萄糖代谢的横断面和前瞻性关系:一项 KORA F4/FF4 研究。

Cross-sectional and prospective relationships of endogenous progestogens and estrogens with glucose metabolism in men and women: a KORA F4/FF4 Study.

机构信息

Institute of of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, München-Neuherberg, Germany.

Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), Ludwig-Maximilians-Universität (LMU), München, Germany.

出版信息

BMJ Open Diabetes Res Care. 2021 Feb;9(1). doi: 10.1136/bmjdrc-2020-001951.

Abstract

INTRODUCTION

Relationships between endogenous female sex hormones and glycemic traits remain understudied, especially in men. We examined whether endogenous 17α-hydroxyprogesterone (17-OHP), progesterone, estradiol (E2), and free estradiol (fE2) were associated with glycemic traits and glycemic deterioration.

RESEARCH DESIGN AND METHODS

921 mainly middle-aged and elderly men and 390 perimenopausal/postmenopausal women from the German population-based Cooperative Health Research in the Region of Augsburg (KORA) F4/FF4 cohort study were followed up for a median of 6.4 years. Sex hormones were measured at baseline using mass spectrometry. We calculated regression coefficients (β) and ORs with 95% CIs using multivariable-adjusted linear and logistic regression models for Z-standardized hormones and glycemic traits or glycemic deterioration (ie, worsening of categorized glucose tolerance status), respectively.

RESULTS

In the cross-sectional analysis (n=1222 men and n=594 women), in men, 17-OHP was inversely associated with 2h-glucose (2hG) (β=-0.067, 95% CI -0.120 to -0.013) and fasting insulin (β=-0.074, 95% CI -0.118 to -0.030), and positively associated with Quantitative Insulin Sensitivity Check Index (QUICKI) (β=0.061, 95% CI 0.018 to 0.105). Progesterone was inversely associated with fasting insulin (β=-0.047, 95% CI -0.088 to -0.006) and positively associated with QUICKI (β=0.041, 95% CI 0.001 to 0.082). E2 was inversely associated with fasting insulin (β=-0.068, 95% CI -0.116 to -0.020) and positively associated with QUICKI (β=0.059, 95% CI 0.012 to 0.107). fE2 was positively associated with glycated hemoglobin (HbA) (β=0.079, 95% CI 0.027 to 0.132). In women, 17-OHP was positively associated with fasting glucose (FG) (β=0.068, 95% CI 0.014 to 0.123). fE2 was positively associated with FG (β=0.080, 95% CI 0.020 to 0.141) and HbA (β=0.121, 95% CI 0.062 to 0.180). In the sensitivity analyses restricted to postmenopausal women, we observed a positive association between 17-OHP and glycemic deterioration (OR=1.518, 95% CI 1.033 to 2.264).

CONCLUSIONS

Inter-relations exist between female sex hormones and glucose-related traits among perimenopausal/postmenopausal women and insulin-related traits among men. Endogenous progestogens and estrogens appear to be involved in glucose homeostasis not only in women but in men as well. Further well-powered studies assessing causal associations between endogenous female sex hormones and glycemic traits are warranted.

摘要

简介

内源性女性性激素与血糖特征之间的关系仍未得到充分研究,尤其是在男性中。我们研究了 17α-羟孕酮(17-OHP)、孕酮、雌二醇(E2)和游离雌二醇(fE2)是否与血糖特征和血糖恶化有关。

研究设计和方法

来自德国基于人群的奥格斯堡合作健康研究(KORA)F4/FF4 队列研究的 921 名主要为中老年人和 390 名围绝经期/绝经后妇女在中位随访 6.4 年后进行了研究。基线时使用质谱法测量性激素。我们使用多变量调整的线性和逻辑回归模型,分别为 Z 标准化激素和血糖特征或血糖恶化(即分类的葡萄糖耐量状态恶化)计算回归系数(β)和比值比(OR)及其 95%置信区间。

结果

在横断面分析(n=1222 名男性和 n=594 名女性)中,在男性中,17-OHP 与 2 小时葡萄糖(2hG)呈负相关(β=-0.067,95%置信区间-0.120 至-0.013)和空腹胰岛素(β=-0.074,95%置信区间-0.118 至-0.030),与定量胰岛素敏感性检查指数(QUICKI)呈正相关(β=0.061,95%置信区间 0.018 至 0.105)。孕酮与空腹胰岛素呈负相关(β=-0.047,95%置信区间-0.088 至-0.006),与 QUICKI 呈正相关(β=0.041,95%置信区间 0.001 至 0.082)。E2 与空腹胰岛素呈负相关(β=-0.068,95%置信区间-0.116 至-0.020),与 QUICKI 呈正相关(β=0.059,95%置信区间 0.012 至 0.107)。fE2 与糖化血红蛋白(HbA)呈正相关(β=0.079,95%置信区间 0.027 至 0.132)。在女性中,17-OHP 与空腹血糖(FG)呈正相关(β=0.068,95%置信区间 0.014 至 0.123)。fE2 与 FG(β=0.080,95%置信区间 0.020 至 0.141)和 HbA(β=0.121,95%置信区间 0.062 至 0.180)呈正相关。在仅包括绝经后妇女的敏感性分析中,我们观察到 17-OHP 与血糖恶化之间存在正相关(OR=1.518,95%置信区间 1.033 至 2.264)。

结论

绝经后/绝经后妇女的女性性激素与血糖特征之间以及男性的胰岛素相关特征之间存在相互关系。内源性孕激素和雌激素似乎不仅在女性中,而且在男性中也参与了血糖稳态。需要进一步进行评估内源性女性性激素与血糖特征之间因果关系的大型研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36c6/7880095/89ca35395998/bmjdrc-2020-001951f01.jpg

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